Associated Papers
Whole exome sequencing identifies KCNH7 variants associated with epilepsy in children.
Wu F et al.
Genes & Diseases, 2025
Purkinje cell hyperexcitability and depressive-like behavior in mice lacking erg3 (ether-à-go-go-related gene) K+ channel subunits.
Schwarz JR et al.
Science Advances, 2024
Development of a Novel Next-Generation Sequencing Assay for Carrier Screening in Old Order Amish and Mennonite Populations of Pennsylvania.
Crowgey EL et al.
The Journal of Molecular Diagnostics : Jmd, 2019
31028937 (PubMed )
Supplement: mmc1.xlsx › SuppTable1_VariantsPanel
Association Study of KCNH7 Polymorphisms and Individual Responses to Risperidone Treatment in Schizophrenia.
Wang X et al.
Frontiers in Psychiatry, 2019
Exome sequencing in large, multiplex bipolar disorder families from Cuba.
Maaser A et al.
Plos One, 2018
Finding Rare, Disease-Associated Variants in Isolated Groups: Potential Advantages of Mennonite Populations.
Lopes FL et al.
Human Biology, 2016
Whole genome/exome sequencing in mood and psychotic disorders.
Kato T
Psychiatry and Clinical Neurosciences, 2015
A population-based study of KCNH7 p.Arg394His and bipolar spectrum disorder.
Strauss KA et al.
Human Molecular Genetics, 2014
Genomic view of bipolar disorder revealed by whole genome sequencing in a genetic isolate.
Georgi B et al.
Plos Genetics, 2014
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